Determination of the enantiomeric excess of chiral carboxylic acids by 31P NMR with C2 symmetrical diamines

Alexakis, Alexandre; Chauvin, Anne-Sophie

doi:10.1016/S0957-4166(01)00257-9

Scientific article

English

Determination of the enantiomeric excess of chiral carboxylic acids by 31P NMR with C2 symmetrical diamines

ContributorsAlexakis, Alexandre; Chauvin, Anne-Sophie

Published inTetrahedron: asymmetry, vol. 12, no. 10, p. 1411-1415

Publication date2001

Abstract

The use of organophosphorus derivatisation agents prepared from C2 symmetric diamines for the 31P NMR determination of the enantiomeric composition of chiral carboxylic acids is described.

Affiliation entities

Faculté des sciences / Section de chimie et biochimie / Département de chimie organique

Citation (ISO format)

ALEXAKIS, Alexandre, CHAUVIN, Anne-Sophie. Determination of the enantiomeric excess of chiral carboxylic acids by 31P NMR with C2 symmetrical diamines. In: Tetrahedron: asymmetry, 2001, vol. 12, n° 10, p. 1411–1415. doi: 10.1016/S0957-4166(01)00257-9

Article (Published version)

Identifiers

PID : unige:8049
DOI : 10.1016/S0957-4166(01)00257-9

Journal ISSN0957-4166

611views

0downloads

Creation21/06/2010 14:15:52

First validation21/06/2010 14:15:52

Update time14/03/2023 15:47:51

Status update14/03/2023 15:47:51

Last indexation10/06/2025 21:36:01

Archive ouverte UNIGE

Determination of the enantiomeric excess of chiral carboxylic acids by 31P NMR with C2 symmetrical diamines

The use of organophosphorus derivatisation agents prepared from C2 symmetric diamines for the 31P NMR determination of the enantiomeric composition of chiral carboxylic acids is described.

Technical informations